0 110Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0Others0Total1Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 35,657 White British ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 4 × 10−11.
How common The G allele had a frequency of about 49% in the people studied.
Where it sits Chromosome 1, band 1q42.13 — in an intron of WNT3A.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Cortical thickness — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Cortical thickness.
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Cortical thickness compared to the general population.
rs1745416 is a single position in the genome, in or near the WNT3A gene. Published research associates it with cortical thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1745416 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs1745416 come from?
GWAS Catalog, NeuroImage 2021, PMID:34560273. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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